Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467104Generated: October 27, 2026

m-Chloroperbenzoic acid → 6-Methanesulphonamido-2-methylquinoline-1-oxide

https://huagongshe.com/reaction/467104

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantN-(2-Methylquinolin-6-yl)methanesulfonamideHCID 19813426—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product6-Methanesulphonamido-2-methylquinoline-1-oxideHCID 19813436—

Reaction Steps

m-Chloroperbenzoic acid ("MCPBA") (5.2 g) was added portionwise to a solution of 6-methanesulphonamido-2-methylquinoline (6 g) in methylene chloride and stirring was continued for 17 hours. The reaction mixture was then diluted with aqueous sodium bicarbonate and the organic layer was separated. The aqueous layer was extracted with methylene chloride. The combined organic layers were washed with aqueous sodium bicarbonate, dried (MgSO4) and evaporated in vacuo to give a solid which was recrystallised from ethanol to give the title compound, yield 1.6 g, m.p. 241°-243°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05158964
Source datasetuspto-grants-1992_10
ORD IDord-d93894f0ebc546c89f1b63da77f6b7af
Source noteuspto-grants-1992_10